Skip to main content
Plant Physiology logoLink to Plant Physiology
. 1978 Mar;61(3):402–405. doi: 10.1104/pp.61.3.402

Effects of Irradiance during Growth on Adaptive Photosynthetic Characteristics of Velvetleaf and Cotton 1

David T Patterson 1, Stephen O Duke 1, Robert E Hoagland 1
PMCID: PMC1091877  PMID: 16660302

Abstract

We grew velvetleaf (Abutilon theophrasti Medic.) and cotton (Gossypium hirsutum L. var. Stoneville 213) at three irradiances and determined the photosynthetic responses of single leaves to a range of six irradiances from 90 to 2000 μeinsteins m−2sec−1. In air containing 21% O2, velvetleaf and cotton grown at 750 μeinsteins m−2sec−1 had maximum photosynthetic rates of 18.4 and 21.9 mg of CO2 dm−2hr−1, respectively. Maximum rates for leaves grown at 320 and 90 μeinsteins m−2sec−1 were 15.3 and 10.3 mg of CO2 dm−2hr−1 in velvetleaf and 12 and 6.7 mg of CO2 dm−2hr−1 in cotton, respectively. In 1 O2, maximum photosynthetic rates were 1.5 to 2.3 times the rates in air containing 21% O2, and plants grown at medium and high irradiance did not differ in rate. In both species, stomatal conductance was not significantly affected by growth irradiance. The differences in maximum photosynthetic rates were associated with differences in mesophyll conductance. Mesophyll conductance increased with growth irradiance and correlated positively with mesophyll thickness or volume per unit leaf area, chlorophyll content per unit area, and photosynthetic unit density per unit area. Thus, quantitative changes in the photosynthetic apparatus help account for photosynthetic adaptation to irradiance in both species. Net assimilation rates calculated for whole plants by mathematical growth analysis were closely correlated with single-leaf photosynthetic rates.

Full text

PDF
402

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Arnon D. I. COPPER ENZYMES IN ISOLATED CHLOROPLASTS. POLYPHENOLOXIDASE IN BETA VULGARIS. Plant Physiol. 1949 Jan;24(1):1–15. doi: 10.1104/pp.24.1.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Björkman O. Comparative studies on photosynthesis in higher plants. Photophysiology. 1973;8:1–63. doi: 10.1016/b978-0-12-282608-5.50007-2. [DOI] [PubMed] [Google Scholar]
  3. Ecklund P. R., Moore T. C. Correlations of Growth Rate and De-etiolation with Rate of Ent-Kaurene Biosynthesis in Pea (Pisum sativum L.). Plant Physiol. 1974 Jan;53(1):5–10. doi: 10.1104/pp.53.1.5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Kanemasu E. T., Thurtell G. W., Tanner C. B. Design calibration and field use of a stomatal diffusion porometer. Plant Physiol. 1969 Jun;44(6):881–885. doi: 10.1104/pp.44.6.881. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Nobel P. S. Photosynthetic Rates of Sun versus Shade Leaves of Hyptis emoryi Torr. Plant Physiol. 1976 Aug;58(2):218–223. doi: 10.1104/pp.58.2.218. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Nobel P. S., Zaragoza L. J., Smith W. K. Relation between Mesophyll Surface Area, Photosynthetic Rate, and Illumination Level during Development for Leaves of Plectranthus parviflorus Henckel. Plant Physiol. 1975 Jun;55(6):1067–1070. doi: 10.1104/pp.55.6.1067. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Shiozawa J. A., Alberte R. S., Thornber J. P. The P700-chlorophyll a-protein. Isolation and some characteristics of the complex in higher plants. Arch Biochem Biophys. 1974 Nov;165(1):388–397. doi: 10.1016/0003-9861(74)90177-5. [DOI] [PubMed] [Google Scholar]

Articles from Plant Physiology are provided here courtesy of Oxford University Press

RESOURCES